Janitex Antibacterial Wet Wipes
FDA Label NDC 79519-050

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Pacific Health Systems Inc. for the product Janitex Antibacterial Wet Wipes (NDC 79519-050). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding drug facts, active ingredients, purpose, uses, warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Benzalkonium Chloride (0.1%)

Purpose

Antiseptic

Uses

  • To decrease bacteria on the skin that could cause disease

Warnings

  • For external use only, harmful if swallowed.
  • Do not use as baby wipe.
  • Do not flush.
  • Do not use on open skin wounds.
  • Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
  • Stop use and ask a doctor if irritation or allergic reaction occurs.
  • Flammable - Keep away from fire or flame

Directions

• Open lid, gently peel back resealable label, remove and use wipes as required. Keep lid closed to prevent moisture loss.

• No need to rinse after usage. Allow skin to dry without wiping. • For adults and children 2 years and over. Discard properly after use. • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store in dry and cool place and away from oxidizers.

Inactive Ingredients

Aqua, Phenoxyethanol, Propylene Glycol, Parfum, Cocamidopropyl Betaine, PEG-40 Hydrogenated Castor Oil, Benzoic Acid, Tetrasodium EDTA, Dehydroacetic Acid, Sodium Hydroxide

Packaging

Image (79519050lb)

Image (79519050lb)

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